참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | Bromine | HCID 24408 | — |
| 반응물 | Methyl 3-nitrobenzoate | HCID 69260 | — |
| 촉매 | Sulfuric Acid | HCID 1118 | — |
| 촉매 | HCID 178418844 | HCID 178418844 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | Methyl 3-bromo-5-nitrobenzoate | HCID 239341 | 72% |
반응 단계
A mixture of methyl 3-nitrobenzoate (122 g, 674 mmol), silver sulphate (100 g, 320.7 mmol) and concentrated sulfuric acid (750 mL) was stirred mechanically and heated at 90° C. To this mixture was added bromine (37 mL), dropwise, over 2 h. The reaction was stirred another hour, cooled and filtered. The filtrate was mixed with 2 L water and 1 Kg crushed ice. The solid was filtered and dried to afford a mixture of the desired methyl ester and free acid hydrolysis product. The mixture was taken up into methanol (1 L), treated with 10 drops concentrated sulfuric acid and refluxed for 12 h. The reaction mixture was allowed to cool and the crystals that were deposited were collected and dried in a desiccator to afford 126 g (72% yield) of methyl 3-bromo-5-nitrobenzoate (EX-119A): 1H NMR (300 MHz, CDCl3) δ 8.65 (s, 1H), 8.44 (s, 1H), 8.37 (s, 1H), 3.94 (s, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07119094B1 |
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| 출처 데이터셋 | uspto-grants-2006_10 |
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| ORD ID | ord-19b2dd6100e14109b7c4f2fb640df9d7 |
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| 출처 메모 | uspto-grants-2006_10 |
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